Camber Spine Technologies FDA Approvals

0 new drug approvals and 6 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
SPIRA® Anterior Lumbar Spacers510(k)Jul 12, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jul 12, 2024
Camber Sacroiliac (SI) Fixation System510(k)Feb 27, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 27, 2024
SPIRA® Posterior Lumbar Spacers510(k)Jul 11, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jul 11, 2023
ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)510(k)Mar 30, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 30, 2023
SPIRA®-C Integrated Fixation System510(k)Mar 22, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Mar 22, 2023
Camber Spine Navigation System510(k)Apr 29, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Apr 29, 2022